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2,5-Difluoroaniline

    • Product Name 2,5-Difluoroaniline
    • Alias 2,5-Difluorobenzenamine
    • Einecs 219-257-0
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    926794

    Cas Number 367-25-9
    Molecular Formula C6H5F2N
    Molecular Weight 129.11
    Appearance Colorless to pale yellow liquid
    Melting Point -7 °C
    Boiling Point 180-182 °C
    Density 1.27 g/cm³
    Refractive Index 1.549
    Solubility In Water Slightly soluble
    Purity Typically ≥98%
    Flash Point 65 °C
    Synonyms 2,5-Difluorobenzenamine
    Smiles c1cc(N)ccc1F

    As an accredited 2,5-Difluoroaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 2,5-Difluoroaniline is packaged in a sealed 100g amber glass bottle with a secure screw cap and safety labeling.
    Shipping 2,5-Difluoroaniline should be shipped in tightly sealed containers, clearly labeled, and handled according to standard chemical shipping regulations. It requires transport in compliance with local, national, and international regulations for hazardous materials, ensuring protection from physical damage, moisture, and extreme temperatures. Appropriate documentation and safety data must accompany the shipment.
    Storage 2,5-Difluoroaniline should be stored in a cool, dry, well-ventilated area, away from incompatible substances such as strong oxidizers and acids. Keep the container tightly closed and protected from light. Store in a chemical-resistant, clearly labeled container. Avoid sources of ignition and excessive heat. Use appropriate personal protective equipment when handling or transferring the material.
    Application of 2,5-Difluoroaniline

    Applications of 2,5-Difluoroaniline in Industrial Manufacturing

    2,5-Difluoroaniline serves as a critical intermediate in a range of advanced industrial production settings. Our manufacturing processes focus on maintaining high purity and consistent quality to meet the precise demands of downstream sectors. Below, we outline key application scenarios and associated compliance, formulation, process, and product details for industrial partners.

    1. Pharmaceutical Intermediate for Fluorinated Drug Synthesis

    Producers in the pharmaceutical sector employ this material as a building block for synthesizing APIs in segments such as anti-infectives, central nervous system agents, and oncology drugs. The fluoro-substitution enhances metabolic stability and bioavailability in final compounds. End-users introduce 2,5-difluoroaniline during the early stages of multi-step reactions including nucleophilic aromatic substitution and amide coupling, especially for creating fluorinated aniline motifs found in patented pharmaceuticals.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 (US FDA cGMP)
    • European Pharmacopeia reference standards for impurity controls
    • REACH Regulation (1907/2006/EC) preregistration

    Typical usage ratio

    • 5–25 mol% relative to target API molecule, adjustable based on reaction design and desired yield

    Downstream process integration

    • Multi-step API synthesis, typically as the starting arylamine for fluorinated core introduction or substituted aromatic amide formation
    • Direct input into halogenation, coupling, or condensation reactions under controlled pH and temperature

    Final product types

    • Fluorinated APIs (e.g., antitumor agents, CNS pharmaceuticals)
    • Advanced pharmaceutical intermediates for late-stage development

    2. Agrochemical Active Ingredient Manufacturing

    The agrochemical sector incorporates 2,5-difluoroaniline as a precursor for selective herbicides, fungicides, and insecticidal actives. Its fluorinated aromatic structure confers resistance to metabolic degradation in crop protection chemicals, thereby improving environmental persistence profiles and spectrum of activity. Our product enters at the coupling or substitution stages for the construction of fluorinated azole or aniline derivative pesticides.

    Industry compliance standards

    • FAO/WHO specifications for pesticide technical materials
    • ISO 9001:2015 Quality Management for production batches
    • Regulation (EC) No 1107/2009 (EU Plant Protection Products Regulation)
    • US EPA Pesticide Registration (FIFRA)

    Typical usage ratio

    • 10–30% by weight in active ingredient synthesis batches, adjusted for formulation scale and reaction pathway

    Downstream process integration

    • Early-stage intermediate for building fluorinated aromatic rings via nucleophilic or electrophilic aromatic substitution
    • Condensation with triazole or phenoxyacetic acid scaffolds

    Final product types

    • Fluorinated herbicides and fungicides (e.g., difluoroanilines, triazole ring compounds)
    • Custom pesticide intermediates for proprietary formulations

    3. Specialty Dye and Pigment Synthesis

    Manufacturers in the specialty colorants sector rely on 2,5-difluoroaniline for synthesizing high-performance dyes and pigments with specific lightfastness and chemical resistance. The incorporation of difluoroaniline into azo, anthraquinone, or phthalocyanine chromophores enhances stability and hue modulation, particularly for fiber, ink, and paint formulations targeted at high-value markets.

    Industry compliance standards

    • ISO 9073-2 for color fastness testing
    • OEKO-TEX Standard 100 for restricted substances in textiles
    • EN 71-3 (Safety of Toys — Migration of Certain Elements) for pigments in children’s products
    • ASTM D4828 for pigment identification

    Typical usage ratio

    • 15–40% of total amine content in dye intermediate synthesis, selected based on target chromophore class and absorption spectrum

    Downstream process integration

    • Primary input for diazotization to form azo dyes or for direct condensation in phthalocyanine pigment frameworks
    • Inclusion at the colorant pre-synthesis or modification step for improved molecular properties

    Final product types

    • Reactive textile dyes
    • Industrial pigments for coatings and plastics
    • Specialty inks for digital printing

    4. Electronic and High-Performance Polymer Manufacture

    Producers of polymers for electronics and engineering applications integrate this material in the backbone of polyimides, polyamides, and specialty resins. The difluorinated aromatic amine provides advantages such as greater thermal stability, lower dielectric constant, and enhanced chemical inertness, critical for flexible circuits and advanced insulation materials.

    Industry compliance standards

    • UL 94 for flammability ratings of polymeric materials
    • RoHS Directive (2011/65/EU) for restricted substances
    • IEC 60216 for thermal endurance of electrical insulating materials
    • ISO 9001:2015 for manufacturing quality management

    Typical usage ratio

    • 5–20 mol% in aromatic diamine monomer mixes, with adjustments for target polymer architecture and specific electronic properties

    Downstream process integration

    • Entry as a functional monomer during polycondensation with dianhydrides or dicarboxylic acids
    • Direct use in solution or melt polymerization setups under controlled inert atmosphere

    Final product types

    • Flexible printed circuit substrates
    • Electronics encapsulants and potting materials
    • Heat-resistant polymer films and resins

    5. Fine Chemical and Custom Synthesis

    In fine chemicals manufacturing, 2,5-difluoroaniline acts as a platform molecule for the introduction of electron-withdrawing fluoroaryl units into target compounds, serving custom synthesis projects in research organizations and specialty OEMs. Its use spans ligands for catalysts, specialty reagents, and unique building blocks for catalog chemicals, supporting rapid development cycles and proprietary molecule production.

    Industry compliance standards

    • ISO 17034 for reference material producers
    • REACH (EU) chemical registration and safety assessment
    • GHS-based SDS documentation requirements
    • Responsible Care® program adherence for chemical manufacture

    Typical usage ratio

    • Varies widely (5–50 mol%) depending on reaction target, scale, and molecular design strategies

    Downstream process integration

    • Direct incorporation at the initial synthesis step for new compound assembly
    • Utilization in substitution, alkylation, or cross-coupling reactions governed by laboratory or pilot protocols

    Final product types

    • Specialty fluorinated ligands and reagents
    • Custom intermediates for contract manufacturing
    • Electronic research-grade chemicals
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